Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single-sided deafness.

bone conduction device contralateral routing of sound randomized controlled trial single‐sided deafness trial period

Journal

Laryngoscope investigative otolaryngology
ISSN: 2378-8038
Titre abrégé: Laryngoscope Investig Otolaryngol
Pays: United States
ID NLM: 101684963

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 25 08 2022
revised: 14 11 2022
accepted: 15 12 2022
entrez: 27 2 2023
pubmed: 28 2 2023
medline: 28 2 2023
Statut: epublish

Résumé

Patients with single-sided deafness (SSD) may experience difficulties with speech perception in noise, sound localization, have tinnitus and experience a reduced quality of life (QoL). contralateral routing of sound hearing aids (CROS) or bone conduction devices (BCD) may partly improve subjective speech communication and QoL in SSD patients. A trial period with these devices can help in making a well-informed choice of treatment. Our aim was to evaluate factors influencing the choice of treatment made after a BCD and CROS trial period in adult SSD patients. Patients were randomized in the: "first BCD, then CROS" or "first CROS, then BCD" trial period group. After the BCD on headband and CROS were tested for 6 weeks each, patients choose for BCD, CROS or no treatment. Primary outcome was the distribution of choice of treatment. Secondary outcomes included the association between the choice of treatment and patient characteristics, reasons for treatment acceptance or rejection, device usage during the trial periods, and disease-specific QoL outcomes. Of 91 patients randomized, 84 completed both trial periods and made their choice of treatment: 25 (30%) BCD, 34 (40%) CROS, and 25 (30%) no treatment. No characteristics were found to be related to choice of treatment. Top three reasons for acceptance or rejection were: device (dis)comfort, sound quality and (dis)advantage of subjective hearing. Average daily device use during the trial periods was higher for CROS than for BCD. Choice of treatment was significantly related with both duration of device usage and greater improvement of QoL after the corresponding trial period. The majority of SSD patients preferred BCD or CROS over no treatment. Evaluating device usage, discussing treatment (dis)advantages and disease-specific QoL outcomes after trial periods are to be considered during patient counseling and could facilitate whether to choose one of these treatments. 1B.

Identifiants

pubmed: 36846432
doi: 10.1002/lio2.1002
pii: LIO21002
pmc: PMC9948587
doi:

Types de publication

Journal Article

Langues

eng

Pagination

192-200

Informations de copyright

© 2022 The Authors. Laryngoscope Investigative Otolaryngology published by Wiley Periodicals LLC on behalf of The Triological Society.

Déclaration de conflit d'intérêts

There are no competing interests for any of the authors. This study is partly funded by Cochlear Ltd. as an unrestricted research grant. By research contract, Cochlear Ltd. did not have influence on the study design, data collection, analysis, data interpretation, and publication.

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Auteurs

Anne W Wendrich (AW)

Department of Otorhinolaryngology and Head & Neck Surgery University Medical Center Utrecht Utrecht Netherlands.
UMC Utrecht Brain Center University Medical Center Utrecht Utrecht Netherlands.

Jan A A van Heteren (JAA)

Department of Otorhinolaryngology and Head & Neck Surgery University Medical Center Utrecht Utrecht Netherlands.
UMC Utrecht Brain Center University Medical Center Utrecht Utrecht Netherlands.

Jeroen P M Peters (JPM)

Department of Otorhinolaryngology and Head & Neck Surgery University Medical Center Utrecht Utrecht Netherlands.
UMC Utrecht Brain Center University Medical Center Utrecht Utrecht Netherlands.

Guido Cattani (G)

Department of Otorhinolaryngology and Head & Neck Surgery University Medical Center Utrecht Utrecht Netherlands.
Adelante Center of Expertise in rehabilitation and Audiology Hoensbroek Netherlands.

Robert J Stokroos (RJ)

Department of Otorhinolaryngology and Head & Neck Surgery University Medical Center Utrecht Utrecht Netherlands.
UMC Utrecht Brain Center University Medical Center Utrecht Utrecht Netherlands.

Huib Versnel (H)

Department of Otorhinolaryngology and Head & Neck Surgery University Medical Center Utrecht Utrecht Netherlands.
UMC Utrecht Brain Center University Medical Center Utrecht Utrecht Netherlands.

Adriana L Smit (AL)

Department of Otorhinolaryngology and Head & Neck Surgery University Medical Center Utrecht Utrecht Netherlands.
UMC Utrecht Brain Center University Medical Center Utrecht Utrecht Netherlands.

Classifications MeSH